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Spinocerebellar ataxias: analysis of CAG expansions at SCA1, SCA 2, SCA 3, and SCA 6 loci in Italian families

✍ Scribed by A. Nardacchione; E. Dragone; L. Orsi; P Mortara; A. Franco; E. Pavanelli; E. Grosso; G. Matullo; A. Carbonara; G. Restagno


Book ID
117670880
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
132 KB
Volume
7
Category
Article
ISSN
0960-8966

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The spinocerebellar ataxias (SCAs) are clinically and genetically a heterogeneous group of neurodegenerative disorders. To date, eight different loci causing SCA have been identified: SCA1, SCA2, Machado-Joseph disease (MJD)/SCA3, SCA4, SCA5, SCA6, SCA7, and dentatorubropallidoluysian atrophy (DRPLA